Neurogenic cervical spondylosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age 18~70 years old male or female; 2) Meet the western medical diagnostic criteria of cervical radiculopathy. 2) Meet the western medical diagnostic criteria for nerve root cervical spondylosis; 3) Meet the diagnostic criteria for Qi stagnation and blood stasis in Chinese medicine; and 1) Age 18~70 years old male or female; 2) Meet the western medical diagnostic criteria of radiculopathy; 3) Meet the diagnostic criteria of qi stagnation and blood stasis of radiculopathy in Chinese medicine. 4) The patient himself/herself or his/her guardian agreed to participate in the study and agreed to participate in the study by signing the informed consent form. 5) Ability to complete the questionnaires and test-related examinations; 6) Normal liver and kidney function; 5) Ability to complete the questionnaires and test-related examinations. 6) Normal liver and kidney function. 7) NRS score =3 or above.
Exclusion criteria
Exclusion criteria: 1) patients with serious heart lung liver kidney and other important organs and blood system function abnormalities; 2) patients with moderate to severe cognitive impairment unable to cooperate with the completion of rehabilitation treatment and examination; patients with severe cognitive impairment unable to cooperate with the completion of rehabilitation treatment and examination 2) Patients with moderate-to-severe cognitive impairment who are unable to cooperate with the completion of rehabilitation treatment and examination; 3) Women who are pregnant or breastfeeding at the same time. (iii) Women who are pregnant or breastfeeding at the same time; (iv) Patients who do not have radicular pain. 4) Patients without radicular pain and patients with pure axial neck pain or spinal cord disease; 5) Patients who are participating in other clinical studies; 6) Patients with skin infections localized at the acupuncture points; 7) Use of medication that interferes with the observation of efficacy within 2 weeks prior to randomization including (fulfilling any of the following). 1) taking aspirin or other non-steroidal anti-inflammatory drugs. 2) Topical application of anti-inflammatory analgesic or blood-stasis activating creams. 3) have done massage physical therapy hot compress treatment. 8) active peptic ulcers / bleeding 9) patients with claustrophobia at the same time
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NRS score improvement rate;Neck Disability Index; | — |
Secondary
| Measure | Time frame |
|---|---|
| SF-36;Inflammation indicators;C2-7SVA\C2-7Cobb\T1-Slope\ROM;fALFF; | — |
Countries
China
Contacts
Dongzhimen Hospital of Beijing University of Chinese Medicine